A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135473



Internal ID19276250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110907067..110907305hg38UCSC Ensembl
Outerchr13:111559414..111559652hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1039n106
Supporting Variantsnssv3989031, nssv3966045
SamplesKWS2, KWS1
Known GenesANKRD10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135473
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer